HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 865347Generated: October 31, 2026
Potassium Permanganate → 5-(4-Cyanobenzyloxy)-2-nitrobenzoic acid
https://huagongshe.com/reaction/865347
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Permanganate | HCID 516875 | — |
| Reactant | 5-(4-Cyanobenzyloxy)-2-nitrobenzaldehyde | HCID 22904973 | — |
| Catalyst | Tetrabutylammonium Bromide | HCID 74236 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Product | 5-(4-Cyanobenzyloxy)-2-nitrobenzoic acid | HCID 22904955 | 125.2% |
Reaction Steps
Potassium permanganate (6.18 g, 39.1 mmol) was added in portions to a stirred solution of 13.8 g (48.9 mmol) of 5-(4-cyanobenzyloxy)-2-nitrobenzaldehyde and 1.58 g (4.89 mmol) of tetrabutylammonium bromide in 70 mL of pyridine. After 1 h, the solvent was removed in vacuo and the residue was partitioned between ethyl acetate and water. Sodium hydrogen sulfite was added to destroy excess permanganate and the aqueous phase was separated and extracted with ethyl acetate. The combined organics were washed with 1N sodium hydrogen sulfate, brine, dried over anhydrous magnesium sulfate, and concentrated to give 14.6 g of 5-(4-cyanobenzyloxy)-2-nitrobenzoic acid as a powder, used without further purification. 1H NMR (300 MHz, d6 -acetone) d 8.07 (1H, d, J=8.8 Hz, O-Ar-H), 7.86 (2H, d, J=8.3 Hz, NC-Ar-H2), 7.78 (2H, d, J=8.3 Hz, NC-Ar-H2), 7.39 (1H, d, J=2.9 Hz, O-Ar-H), 7.36 (1H, dd, J=8.8, 2.9 Hz, O-Ar-H), 5.48 (2H, s, ArCH2O).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05565449 |
|---|
| Source dataset | uspto-grants-1996_10 |
|---|
| ORD ID | ord-99a8a2453a5244a5a7d012ced83e14ed |
|---|
| Source note | uspto-grants-1996_10 |
|---|